Gene Expression: KCNQ2

Gene Data

  • Gene Symbol: KCNQ2
  • Gene ID: 3785
  • Synonyms: BFNC, BFNS1, EBN, EBN1, EIEE7, ENB1, HNSPC, KCNA11, KV7.2, KVEBN1
  • Description: potassium voltage-gated channel, KQT-like subfamily, member 2
  • Database Refs: HGNC:6296, MIM:602235, Ensembl:ENSG00000075043, HPRD:03757, Vega:OTTHUMG00000033049
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 5 out of 21 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters:

Disease Associations

This gene is associated with the following diseases. Clicking on the disease will take you to the disease association entry for that disease.

This gene is associated with 28 diseases, scroll to view all:
  1. Benign familial neonatal convulsion
  2. Benign neonatal epilepsy
  3. Brain disease
  4. Central nervous system disease
  5. Complex genetic disease
  6. Developmental disease of mental health
  7. Disease
  8. Disease of anatomical entity
  9. Disease of mental health
  10. Epilepsy
  11. Episodic ataxia
  12. Generalized epilepsy
  13. Infantile epileptic encephalopathy
  14. Intellectual disability
  15. Long QT syndrome
  16. Migraine
  17. Muscle tissue disease
  18. Muscular disease
  19. Musculoskeletal system disease
  20. Myopathy
  21. Nervous system disease
  22. Neuromuscular disease
  23. Neuropathy
  24. Partial epilepsy
  25. Rolandic epilepsy
  26. Specific developmental disease
  27. Unverricht-Lundborg syndrome
  28. West syndrome

Stage Associations

This gene is associated with the following stages: